ACOT9

acyl-CoA thioesterase 9
OMIM: 300862, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red ACOT9 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 3.3
Signed off v.3.2 on 13 Feb 2020

Component of the following Super Panels:

  • Hypotonic infant
  • Paediatric disorders
  • White matter disorders - childhood onset
  • review Unknown
    Sources
    • Expert Review Red
    Phenotypes
    • Intellectual disability